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Titlebook: Immune Checkpoint Blockade; Methods and Protocol Yago Pico de Coa?a Book 2019 Springer Science+Business Media, LLC, part of Springer Nature

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書目名稱Immune Checkpoint Blockade
副標(biāo)題Methods and Protocol
編輯Yago Pico de Coa?a
視頻videohttp://file.papertrans.cn/463/462041/462041.mp4
概述Includes cutting-edge techniques.Provides step-by-step detail essential for reproducible results.Contains key implementation advice from the experts
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Immune Checkpoint Blockade; Methods and Protocol Yago Pico de Coa?a Book 2019 Springer Science+Business Media, LLC, part of Springer Nature
描述This detailed volume describes a series of techniques that are essential for evaluating the efficacy of new checkpoint blockade therapies as well as understanding the mechanisms behind the therapies that have already been approved. Beginning with a section on describing the tumor microenvironment and evaluating the immune system at a systemic level, the book continues by covering functional assays that provide answers to questions that may be raised after studying the immune system and its responses to immunotherapies, as well as the use of animal models in this research. Written for the highly successful .Methods in Molecular Biology. series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.?.Authoritative and practical, .Immune Checkpoint Blockade: Methods and Protocols. serves to aid researchers in furthering our understanding of checkpoint blockage as well as the study of tumor immunology and the development of new immunotherapies..
出版日期Book 2019
關(guān)鍵詞Tumor immunology; Immunotherapy; Antitumoral immune responses; Functional assays; Cancer cell lines; Tran
版次1
doihttps://doi.org/10.1007/978-1-4939-8979-9
isbn_ebook978-1-4939-8979-9Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media, LLC, part of Springer Nature 2019
The information of publication is updating

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Systems-Level Immune Monitoring by Mass Cytometry immune responses in human patients are needed. Mass cytometry allows for detailed profiling of all immune cell populations and their functional responses using a simple blood sample. When combined with appropriate computational analyses, the resolution for distinguishing desired responses from unpr
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Immune Monitoring of Cancer Patients by Multi-color Flow Cytometryo these novel treatments. Multicolor flow cytometry is a powerful tool that enables tumor immunologists to characterize the immune system of patients before and in response to immunotherapy. We present here a protocol for purifying human peripheral blood mononuclear cells and staining them with a se
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High-Throughput, Fast, and Sensitive Immunopeptidomics Sample Processing for Mass Spectrometryand other diseases. So far, methodologies for recovery of HLA class I and II peptides for subsequent mass spectrometry-based analysis have been a major limitation. In this chapter we describe a detailed protocol for a high-throughput, reproducible, and sensitive immunoaffinity-purification of HLA-I
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Expansion of Tumor-Infiltrating Lymphocytes from Melanoma Tumorsom tumors is usually performed in two steps. The details of the procedure differ between different laboratories, but the general concept remains the same. In the first step, small fragments of a tumor are placed in culture medium containing one or more T cell stimulating growth factors. Here the mos
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Establishment of Two Dimensional (2D) and Three-Dimensional (3D) Melanoma Primary Cultures as a Toolottom of plastic flasks. Melanoma cells can be cultured with a considerable degree of success, and, depending on the further use of the cells obtained in the culture, methodologies have to be adjusted to obtain reliable results. Although there are many melanoma continuous cell lines, in vitro 2D and
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Expansion and Determination of Antigen-Reactive T Cells by Flow Cytometryt these cells face major limitations, like the predetermination of the given HLA type. The herein described protocol provides a means of overcoming many of the obstacles associated with the use of multimers and other common approaches in this field. In order to be able to detect rare cells which are
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